Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 074976
Company: MYLAN

Products on ANDA 074976

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
ACYCLOVIR	ACYCLOVIR	400MG	TABLET;ORAL	Discontinued	None	No	No
ACYCLOVIR	ACYCLOVIR	800MG	TABLET;ORAL	Discontinued	None	No	No

Approval Date(s) and History, Letters, Labels, Reviews for ANDA 074976

Original Approvals or Tentative Approvals

Action Date	Submission	Action Type	Submission Classification	Review Priority; Orphan Status	Letters, Reviews, Labels, Patient Package Insert	Notes	Url
04/13/1998	ORIG-1	Approval			Label Letter Review		https://www.accessdata.fda.gov/drugsatfda_docs/anda/98/74-976_Acyclovir.htm https://www.accessdata.fda.gov/drugsatfda_docs/anda/98/74-976_Acyclovir.htm https://www.accessdata.fda.gov/drugsatfda_docs/anda/98/74-976_Acyclovir.cfm

Supplements

Action Date	Submission	Supplement Categories or Approval Type	Letters, Reviews, Labels, Patient Package Insert	Note	Url
09/12/2000	SUPPL-2	Labeling		Label is not available on this site.
12/20/1999	SUPPL-1	Manufacturing (CMC)		Label is not available on this site.

Labels for ANDA 074976

Action Date	Submission	Supplement Categories or Approval Type	Letters, Reviews, Labels, Patient Package Insert	Note	Url
04/13/1998	ORIG-1	Approval			https://www.accessdata.fda.gov/drugsatfda_docs/anda/98/74-976_Acyclovir.htm